Common variable immunodeficiency (CVID) and inclusion body myositis (IBM)

Angela Gause; Daniela Christine Inderrieden; Rudolf Laas; Andreas Christoph Arlt; Wolfgang Ludwig Gross

doi:10.1016/S0171-2985(00)80067-4

Common variable immunodeficiency (CVID) and inclusion body myositis (IBM)

Angela Gause^*, Daniela Christine Inderrieden, Rudolf Laas, Andreas Christoph Arlt, Wolfgang Ludwig Gross

^*Corresponding author for this work

Clinic of Rheumatology

7 Citations (Scopus)

Abstract

A case of a 38-year old man with a common variable immunodeficiency syndrome (CVID) is demonstrated who suffered at the same time from a histologically proven inclusion body myositis (IBM). The myositis did not resolve after institution of regular intravenous IgG infusions. This case demonstrates a very long lasting benign course of IBM. The occurrence with CVID may be a clinical hint for a viral pathogenesis of IBM. So far only two similar cases are reported in the literature.

Original language	English
Article number	80067
Journal	Immunobiology
Volume	202
Issue number	2
Pages (from-to)	199-203
Number of pages	5
ISSN	0171-2985
DOIs	https://doi.org/10.1016/S0171-2985(00)80067-4
Publication status	Published - 08.2000

Research Areas and Centers

Academic Focus: Center for Infection and Inflammation Research (ZIEL)

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1016/S0171-2985(00)80067-4

Cite this

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abstract = "A case of a 38-year old man with a common variable immunodeficiency syndrome (CVID) is demonstrated who suffered at the same time from a histologically proven inclusion body myositis (IBM). The myositis did not resolve after institution of regular intravenous IgG infusions. This case demonstrates a very long lasting benign course of IBM. The occurrence with CVID may be a clinical hint for a viral pathogenesis of IBM. So far only two similar cases are reported in the literature.",

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AU - Gross, Wolfgang Ludwig

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AB - A case of a 38-year old man with a common variable immunodeficiency syndrome (CVID) is demonstrated who suffered at the same time from a histologically proven inclusion body myositis (IBM). The myositis did not resolve after institution of regular intravenous IgG infusions. This case demonstrates a very long lasting benign course of IBM. The occurrence with CVID may be a clinical hint for a viral pathogenesis of IBM. So far only two similar cases are reported in the literature.

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Common variable immunodeficiency (CVID) and inclusion body myositis (IBM)

Abstract

Research Areas and Centers

UN SDGs

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